FDA 510(k) Clearance for DJO’s Exprt Revision Hip
DJO Global announced FDA 510(k) clearance to market the Exprt® Revision Hip. Mar 15, 2017
Expanded FDA 510(k) for First Ray Stealth Staple
First Ray received FDA 510(k) clearance for additional sizes and materials in the Stealth Staple™ line. Mar 15, 2017
Arthrosurface to Launch Inlay Glenoid for OVO Primary Stemless Total Shoulder
Within 2017, Arthrosurface plans commercial EU launch of an inlay glenoid component for the OVO™ primary stemless total shoulder. Mar 15, 2017
Soft Tissue Regeneration Raises Series C Financing, Rebrands as Biorez
Soft Tissue Regeneration closed a US $1.5MM Series C Financing and rebranded as Biorez. Mar 15, 2017
DePuy Synthes Launches ATTUNE Knee Revision Options
DePuy Synthes launched the ATTUNE® Revision Fixed Bearing Tibial Base and 14x50mm Cemented Stem. Mar 15, 2017
Study Results: Rotation Medical Bioinductive Implant in Rotator Cuff Tears
Study results indicate that Rotation Medical’s collagen-based Bioinductive Implant induced new tissue formation in all study participants with large and massive rotator cuff tears. Mar 15, 2017
Study Results: Mesoblast’s Cell Therapy in Degenerative Disc Disease
Studies suggest that a single injection of Mesenchymal Precursor Cells resulted in meaningful improvements in chronic low back pain and function that were durable for at least 3 years. Mar 15, 2017
First Fibroblast Injection in Trial for Spinal Disc Regeneration
SpinalCyte announced the first injection in a clinical trial of CybroCell fibroblasts for spinal disc regeneration. Mar 14, 2017
FDA 510(k) Clearance for Kyphon Xpede Bone Cement
Medtronic received FDA 510(k) clearance of Kyphon™ Xpede Bone Cement for fixation of pathological fractures of the sacral ala using sacroplasty. Mar 14, 2017
Study Results: ATTUNE Knee Clinical and Economic Data
Study results demonstrate the clinical and economic value of DePuy Synthes’ ATTUNE® knee in a healthcare environment experiencing cost constraint and growing procedure volumes. Mar 14, 2017
